Canonical Allele Identifier: PA188820
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184389
ClinVar RCV Id: RCV000163638 RCV000198598 RCV000409323 RCV000657088 RCV001706075 RCV003462121 RCV003995266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1334Trp
CA015093
NM_000179.3:c.4000C>T